Cement composition containing a substituted ethoxylated phenol surfactant for use in an oil-contaminated well

ABSTRACT

A well treatment composition comprises a surfactant comprising a substituted ethoxylated phenol having at least one substituent, 1 to 14 moles of ethylene oxide, and the substituent being an alkyl, alkene, or alkyne with a carbon chain length in the range of 4 to 25, wherein the substituted ethoxylated phenol is selected from the group consisting of: ortho-, para-, or meta-substituted ethoxylated phenol; cardanol ethoxylate; derivatives thereof; and combinations of any of the foregoing. Preferably, the surfactant comprises cardanol ethoxylate, a substituted cardanol ethoxylate, and derivatives thereof. A method of cementing in a subterranean formation comprises: introducing a cement composition into the subterranean formation, wherein the cement composition comprises: (A) cement; (B) water; and (C) the surfactant; and allowing the cement composition to set.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional of prior U.S. application Ser. No.12/844,577, filed Jul. 27, 2010.

TECHNICAL FIELD

A well treatment composition containing a surfactant of a substitutedethoxylated phenol is provided. A method of cementing in a subterraneanformation using the surfactant is also provided. In an embodiment, thesubterranean formation is penetrated by a well.

SUMMARY

According to an embodiment, a well treatment composition comprises asurfactant comprising a substituted ethoxylated phenol and derivativesthereof, having at least one substituent, wherein the substitutedethoxylated phenol and derivatives thereof comprises at least one of thefollowing chemical structures:

where n=1-14, R=an alkyl, alkene, or alkyne with a carbon chain lengthin the range of 4 to 25, and where m=0, 2, 4, and 6. According toanother embodiment, the substituted ethoxylated phenol and derivativesthereof, according to the chemical structure identified as IV above, isa substituted cardanol ethoxylate and wherein the substituted cardanolethoxylate and derivatives thereof has at least one of the followingchemical structures:

where n=1-14; m=0, 2, 4, and 6; and R1=an alkyl, alkene, or alkyne witha carbon chain length in the range of 4 to 25.

According to another embodiment, a method of cementing in a subterraneanformation comprises: introducing a cement composition into thesubterranean formation comprising: (A) cement; (B) water; and (C) thesurfactant; and allowing the cement composition to set.

DETAILED DESCRIPTION

As used herein, the words “comprise,” “have,” “include,” and allgrammatical variations thereof are each intended to have an open,non-limiting meaning that does not exclude additional elements or steps.

As used herein, a “fluid” is a substance having a continuous phase thattends to flow and to conform to the outline of its container when thesubstance is tested at a temperature of 71° F. (22° C.) and a pressureof one atmosphere “atm” (0.1 megapascals “MPa”). A fluid can be a liquidor gas. A homogenous fluid has only one phase; whereas a heterogeneousfluid has more than one distinct phase. A colloid is an example of aheterogeneous fluid. A colloid can be: a slurry, which includes acontinuous liquid phase and undissolved solid particles as the dispersedphase; an emulsion, which includes a continuous liquid phase and atleast one dispersed phase of immiscible liquid droplets; or a foam,which includes a continuous liquid phase and a gas as the dispersedphase.

As used herein, the term “water based” means a homogenous fluidcomprising water or a colloid in which the continuous phase compriseswater. As used herein, the term “oil based” means a homogenous fluidcomprising a hydrocarbon liquid or a colloid in which the continuousphase comprises a hydrocarbon liquid. The hydrocarbon liquid can benaturally-occurring or a synthetic liquid.

As used herein, a “cement composition” is a mixture of at least cementand water, and possibly additives. As used herein, the term “cement”means an initially dry substance that, in the presence of water, acts asa binder to bind other materials together. An example of cement isPortland cement. A cement composition is generally a slurry in which thewater is the continuous phase of the slurry and the cement (and anyother insoluble particles) is the dispersed phase. The continuous phasecan include dissolved solids.

Oil and gas hydrocarbons are naturally occurring in some subterraneanformations. A subterranean formation containing oil or gas is sometimesreferred to as a reservoir. A reservoir may be located under land or offshore. Reservoirs are typically located in the range of a few hundredfeet (shallow reservoirs) to a few tens of thousands of feet (ultra-deepreservoirs). In order to produce oil or gas, a wellbore is drilled intoa reservoir or adjacent to a reservoir.

A well can include, without limitation, an oil, gas, water, or injectionwell. As used herein, a “well” includes at least one wellbore. Awellbore can include vertical, inclined, and horizontal portions, and itcan be straight, curved, or branched. As used herein, the term“wellbore” includes any cased, and any uncased, open-hole portion of thewellbore. A near-wellbore region is the subterranean material and rockof the subterranean formation surrounding the wellbore. As used herein,a “well” also includes the near-wellbore region. The near-wellboreregion is generally considered to be the region within about 100 feet ofthe wellbore. As used herein, “into a well” means and includes into anyportion of the well, including into the wellbore or into thenear-wellbore region via the wellbore.

A portion of a wellbore may be an open hole or cased hole. In anopen-hole wellbore portion, a tubing string may be placed into thewellbore. The tubing string allows fluids to be introduced into orflowed from a remote portion of the wellbore. In a cased-hole wellboreportion, a casing is placed into the wellbore which can also contain atubing string. A wellbore can contain an annulus. Examples of an annulusinclude, but are not limited to: the space between the wellbore and theoutside of a tubing string in an open-hole wellbore; the space betweenthe wellbore and the outside of a casing in a cased-hole wellbore; andthe space between the inside of a casing and the outside of a tubingstring in a cased-hole wellbore.

A wellbore is formed using a drill bit. A drill string can be used toaid the drill bit in drilling through the subterranean formation to formthe wellbore. The drill string can include a drilling pipe. Duringdrilling operations, a drilling fluid, sometimes referred to as adrilling mud, may be circulated downwardly through the drilling pipe,and back up the annulus between the wellbore and the outside of thedrilling pipe. The drilling fluid performs various functions, such ascooling the drill bit, maintaining the desired pressure in the well, andcarrying drill cuttings upwardly through the annulus between thewellbore and the drilling pipe.

Generally, drilling fluids are either water based or oil based. Anoil-based drilling fluid can include a synthetic hydrocarbon liquid.Examples of hydrocarbon liquids used in oil-based drilling fluidsinclude, but are not limited to: a fractional distillate of crude oil; afatty derivative of an acid, an ester, an ether, an alcohol, an amine,an amide, or an imide; a saturated hydrocarbon (such as an alkane orparrafin); an unsaturated hydrocarbon (such as an internal olefin); abranched hydrocarbon; and a cyclic hydrocarbon. Commercially-availableexamples of hydrocarbon liquids include, but are not limited to: ENCORE®drilling fluid, BAROID ALKANE™ base fluid, XP-07™ base fluid, andPETROFREE® ESTER base fluid, marketed by Halliburton Energy Services,Inc.; and ESCAID 110™ available from ExxonMobil in Houston, Tex., USA.

Oil-based drilling fluids can provide better shale inhibition, betterlubrication, higher rates of penetration, and deeper bit penetrationcompared to a water-based drilling fluid. Therefore, it is oftendesirable to use an oil-based drilling fluid as opposed to a water-baseddrilling fluid.

During well completion, it is common to introduce a cement compositioninto an annulus in a wellbore. For example, in a cased-hole wellbore, acement composition can be placed into and allowed to set in an annulusbetween the wellbore and the casing in order to stabilize and secure thecasing in the wellbore. By cementing the casing in the wellbore, fluidsare prevented from flowing into the annulus. Consequently, oil or gascan be produced in a controlled manner by directing the flow of oil orgas through the casing and into the wellhead. Cement compositions canalso be used in primary or secondary cementing operations,well-plugging, or gravel packing operations.

It is desirable to remove a drilling fluid completely from a wellborebefore a cement composition is introduced into the wellbore. A spacerfluid can be introduced into the wellbore after the drilling fluid andbefore the cement composition. The spacer fluid can be circulated downthrough a drill string or tubing string and up through an annulus. Thespacer fluid functions to remove the drilling fluid from the wellbore.

Oil-based drilling fluids are generally more difficult to remove with aspacer fluid compared to water-based drilling fluids. As a result, it iscommon for some of an oil-based drilling fluid to remain in the welleven after introducing a spacer fluid into the well. The remainingoil-based drilling fluid is commonly referred to as a “mud-pocket”. Acement composition can mix with some of the remaining oil-based drillingfluid and become “contaminated.” If some of the remaining oil-baseddrilling fluid mixes with the cement composition, then the drillingfluid can cause adverse effects on some of the properties of the cementcomposition. For example, the rheology and compressive strength of thecement composition can be adversely affected.

It has been discovered that a cement composition containing a surfactantof a substituted ethoxylated phenol and derivatives thereof can be usedin a subterranean formation containing an oil-based drilling fluid. Inone embodiment, the substituted ethoxylated phenol is a cardanolethoxylate. The oil-based drilling fluid contaminated cement compositioncontaining the surfactant may exhibit better rheology and a highercompressive strength compared to a contaminated cement compositionwithout the surfactant. Another advantage of the surfactant is that itis compatible with a variety of cement additives. For example, thesurfactant is compatible with Channel Seal™ Fluid, marketed byHalliburton Energy Services, Inc. The surfactant can form a stableemulsion with Channel Seal™ Oil-based Fluid at a temperature of 130° F.(54° C.) for up to 7 days.

A surfactant can increase the water solubility of some hydrophobiccompounds that are poorly soluble in water. A surfactant is amphiphilic,comprising a hydrophobic tail group and a hydrophilic head group. Thehydrophilic head can be charged. A cationic surfactant includes apositively-charged head. An anionic surfactant includes anegatively-charged head. A zwitterionic surfactant includes both apositively- and negatively-charged head. A surfactant with no charge iscalled a non-ionic surfactant.

If a surfactant is in a sufficient concentration in a solution, then thesurfactant molecules can form micelles. A “micelle” is an aggregate ofsurfactant molecules dispersed in a solution. A surfactant in an oilsolution can form reverse-micelles with the hydrophobic tails in contactwith the hydrocarbon solvent, sequestering the hydrophilic heads in thecenter of the reverse-micelle. Conversely, a surfactant in an aqueoussolution can form micelles with the hydrophilic heads in contact withthe surrounding aqueous solvent, sequestering the hydrophobic tails inthe micelle center. The surfactant must be in a sufficient concentrationto form a reverse-micelle or micelle, known as the critical micelleconcentration. The critical micelle concentration is the concentrationof surfactant above which reverse-micelles or micelles are spontaneouslyformed.

When an oil-based drilling fluid is used, it is believed that if thesurfactant, according to the embodiments, is included in a cementcomposition, then the surfactant can sequester some of the hydrocarbonliquid from the oil-based drilling fluid and help prevent thehydrocarbon liquid from contaminating the cement composition. As aresult, some of the adverse effects the hydrocarbon liquid can have onthe cement composition may be diminished.

During cementing operations, it is desirable for the cement compositionto remain pumpable during introduction into the subterranean formationand until the cement composition is situated in the portion of thesubterranean formation to be cemented. After the cement composition hasreached the portion of the subterranean formation to be cemented, thecement composition can ultimately set. A cement composition thatthickens too quickly while being pumped can damage pumping equipment orblock tubing or pipes. A cement composition that sets too slowly cancost time and money while waiting for the composition to set.

If any test (e.g., thickening time or compressive strength) requires thestep of mixing, then the cement composition is “mixed” according to thefollowing procedure. The water is added to a mixing container and thecontainer is then placed on a mixer base. The motor of the base is thenturned on and maintained at 4,000 revolutions per minute (rpm). Thecement and any other ingredients are added to the container at a uniformrate in not more than 15 seconds (s). After all the cement and any otheringredients have been added to the water in the container, a cover isthen placed on the container, and the cement composition is mixed at12,000 rpm (+/−500 rpm) for 35 s (+/−1 s). It is to be understood thatthe cement composition is mixed at ambient temperature and pressure(about 71° F. (22° C.) and about 1 atm (0.1 MPa)).

It is also to be understood that if any test (e.g., thickening time orcompressive strength) requires the test be performed at a specifiedtemperature and possibly a specified pressure, then the temperature andpressure of the cement composition is ramped up to the specifiedtemperature and pressure after being mixed at ambient temperature andpressure. For example, the cement composition can be mixed at 71° F.(22° C.) and 1 atm (0.1 MPa) and then placed into the testing apparatusand the temperature of the cement composition can be ramped up to thespecified temperature. As used herein, the rate of ramping up thetemperature is in the range of about 3° F./min to about 5° F./min (about1.67° C./min to about 2.78° C./min). After the cement composition isramped up to the specified temperature and possibly pressure, the cementcomposition is maintained at that temperature and pressure for theduration of the testing.

As used herein, the “thickening time” is how long it takes for a cementcomposition to become unpumpable at a specified temperature andpressure. The pumpability of a cement composition is related to theconsistency of the composition. The consistency of a cement compositionis measured in Bearden units of consistency (Bc), a dimensionless unitwith no direct conversion factor to the more common units of viscosity.As used herein, a cement composition becomes “unpumpable” when theconsistency of the composition reaches 70 Bc. As used herein, theconsistency of a cement composition is measured as follows. The cementcomposition is mixed. The cement composition is then placed in the testcell of a High-Temperature, High-Pressure (HTHP) consistometer, such asa FANN® Model 275 or a Chandler Model 8240. Consistency measurements aretaken continuously until the cement composition exceeds 70 Bc.

Rheology is a unit-less measure of how a material deforms and flows.Rheology includes the material's elasticity, plasticity, and viscosity.As used herein, the “rheology” of a cement composition is measured asfollows. The cement composition is mixed. The cement composition isplaced into the test cell of a rotational viscometer, such as a FANN®Model 35 viscometer, fitted with a Bob and Sleeve attachment and aspring number 1. The cement composition is tested at the specifiedtemperature and ambient pressure, about 1 atm (0.1 MPa). Rheologyreadings are taken at multiple rpm's, for example, at 3, 6, 30, 60, 100,200, and 300.

A cement composition can develop compressive strength. Cementcomposition compressive strengths can vary from 0 psi to over 10,000 psi(0 to over 69 MPa). Compressive strength is generally measured at aspecified time after the composition has been mixed and at a specifiedtemperature and pressure. Compressive strength can be measured, forexample, at a time of 24 hours. According to ANSI/API RecommendedPractice 10B-2, compressive strength can be measured by either adestructive method or non-destructive method.

The destructive method mechanically tests the compressive strength of acement composition. As used herein, the “destructive compressivestrength” of a cement composition is measured at ambient temperature(about 71° F., about 22° C.) as follows. The cement composition ismixed. The cement composition is then placed into a test cell for atleast 48 hours and a temperature of 220° F. (104° C.) until the cementcomposition has set. The test cell, containing the set cementcomposition is then placed into a compression-testing device, such as aSuper L Universal testing machine model 602, available from TiniusOlsen, Horsham in Pennsylvania, USA. The pressure is gradually increaseduntil the cement composition breaks. The destructive compressivestrength is calculated as the force required to break the sample dividedby the smallest cross-sectional area in contact with the load-bearingplates of the compression-testing device. The destructive compressivestrength is reported in units of pressure, such as pound-force persquare inch (psi) or megapascals (MPa).

The non-destructive method continually measures correlated compressivestrength of a cement composition sample throughout the test period byutilizing a non-destructive sonic device such as an Ultrasonic CementAnalyzer (UCA) available from FANN® Instruments in Houston, Tex., USA.As used herein, the “non-destructive compressive strength” of a cementcomposition is measured at a specified time, temperature, and pressureas follows. The cement composition is mixed. The cement composition isthen placed in an Ultrasonic Cement Analyzer and tested at a specifiedtemperature and pressure. The UCA continually measures the transit timeof the acoustic signal through the sample. The UCA device containspreset algorithms that correlate transit time to compressive strength.The UCA reports the compressive strength of the cement composition inunits of pressure, such as psi or MPa.

The compressive strength of a cement composition can be used to indicatewhether the cement composition has initially set or set. As used herein,a cement composition is considered “initially set” when the cementcomposition develops a compressive strength of 50 psi (0.3 MPa) usingthe non-destructive compressive strength method at a specifiedtemperature and pressure. As used herein, the “initial setting time” isthe difference in time between when the cement and any other ingredientsare added to the water and when the composition is initially set.

As used herein, the term “set,” and all grammatical variations thereof,are intended to mean the process of becoming hard or solid by curing. Asused herein, the “setting time” is the difference in time between whenthe cement and any other ingredients are added to the water and when thecomposition has set at a specified temperature. It can take up to 48hours or longer for a cement composition to set. Some cementcompositions can continue to develop compressive strength over thecourse of several days. The compressive strength of a cement compositioncan reach over 10,000 psi (69 MPa).

As used herein, the “mud contamination” of a cement composition isperformed as follows. An oil-based drilling mud is prepared using aspecified hydrocarbon liquid as the continuous phase of the drillingmud. The cement composition is mixed. A specified percentage by volumeof the drilling mud is hand-mixed with the cement composition using aspatula.

According to an embodiment, a well treatment composition comprises asurfactant comprising a substituted ethoxylated phenol and derivativesthereof, having at least one substituent, wherein the substitutedethoxylated phenol and derivatives thereof comprises at least one of thefollowing chemical structures:

where n=1-14, R=an alkyl, alkene, or alkyne with a carbon chain lengthin the range of 4 to 25, and where m=0, 2, 4, and 6.

According to another embodiment, a cement composition comprises: (A)cement; (B) water; and (C) the surfactant of the well treatmentcomposition.

The discussion of preferred embodiments regarding the well treatmentcomposition, the cement composition, or any ingredient in the welltreatment and cement composition, is intended to apply to thecomposition embodiments and the method embodiments. Any reference to theunit “gallons” means U.S. gallons. As used herein, the term “soluble”means that at least 1 part of the substance dissolves in 99 parts of theliquid at a temperature of 77° F. (25° C.) and a pressure of 1 atm (0.1MPa). As used herein, the term “insoluble” means that less than 1 partof the substance dissolves in 99 parts of the liquid at a temperature of77° F. (25° C.) and a pressure of 1 atm (0.1 MPa).

The cement composition includes cement. The cement can be Class Acement, Class C cement, Class G cement, Class H cement, and anycombination thereof. Preferably, the cement is Class G cement or Class Hcement.

The cement composition includes water. The water can be selected fromthe group consisting of freshwater, brackish water, saltwater, and anycombination thereof. The cement composition can further include awater-soluble salt. Preferably, the salt is selected from sodiumchloride, calcium chloride, calcium bromide, potassium chloride,potassium bromide, magnesium chloride, and any combination thereof. Thecement composition can contain the water-soluble salt in a concentrationin the range of about 5% to about 35% by weight of the water (ww).

The well treatment and cement compositions include a surfactant.According to an embodiment, the surfactant is non-ionic. The surfactantcomprises a substituted ethoxylated phenol and derivatives thereofhaving at least one of the chemical structures identified as numbers Ithrough IV above. The substituted ethoxylated phenol and derivativesthereof can also include combinations of the chemical structuresidentified as numbers I through IV above. The substituted ethoxylatedphenol has at least one substituent. The substituent can beortho-substituted (I), meta-substituted (II), or para-substituted (III).The substituted ethoxylated phenol can include 1 to 14 moles of ethyleneoxide (n=1-14). Preferably, the substituted ethoxylated phenol includes6 to 13 moles of ethylene oxide (n=6-13). According to an embodiment,the surfactant comprises a para-substituted ethoxylated phenolderivative (III) in which R=an alkyl with a carbon chain length of 9(nonyl phenol ethoxylated derivative). The ethoxylated phenol can alsoinclude two or more substituents.

Most preferably, the substituted ethoxylated phenol and derivativesthereof is cardanol ethoxylate (identified as chemical structure numberIV above). Cardanol is naturally-occurring and is a substituted phenolobtained from cashew nutshell liquid (CSNL), a byproduct of cashew nutprocessing. CSNL consists primarily of anacardic acid. Anacardic acidbecomes decarboxylated when heated in the presence of an acid, yieldingthe meta-substituted phenol, cardanol. Cardanol can be ethoxylated toproduce cardanol ethoxylate. Because cardanol ethoxylate isbiodegradable, it can be used in wells where biodegradability isdesired. According to an embodiment, the substituted ethoxylated phenolis a substituted cardanol ethoxylate. According to this embodiment, thesubstituted cardanol ethoxylate is selected from the group consistingof: 6-substituted cardanol ethoxylate (IVa below); 4-substitutedcardanol ethoxylate (IVb below); 5-substituted cardanol ethoxylate (IVcbelow); derivatives of any of the foregoing; and combinations of any ofthe foregoing.

where n=1-14; m=0, 2, 4, and 6; and R₁=an alkyl, alkene, or alkyne witha carbon chain length in the range of 4 to 25.

The substituted ethoxylated phenol can be a derivative of a substitutedethoxylated phenol. An example of a derivative of a substitutedethoxylated phenol is cardanol ethoxylate sulphonate (where R₁=asulphonate according to the chemical structures identified as IVa-IVcabove).

In one embodiment, the surfactant is in a concentration of at least0.05% by weight of the cement (bwc). In another embodiment, thesurfactant is in a concentration in the range of about 0.05% to about 5%bwc. In another embodiment, the surfactant is in a concentration in therange of about 1% to about 3% bwc.

In an embodiment, the cement composition has a thickening time of atleast 3 hours at a temperature of 185° F. (88° C.) and a pressure of17,500 psi (121 MPa). In another embodiment, the cement composition hasa thickening time in the range of about 4 to about 15 hours at atemperature of 185° F. (88° C.) and a pressure of 17,500 psi (121 MPa).Some of the variables that can affect the thickening time of the cementcomposition include the concentration of any set retarder included inthe cement composition, the concentration of any salt present in thecement composition, and the bottomhole temperature of the subterraneanformation. As used herein, the term “bottomhole” refers to the portionof the subterranean formation to be cemented. In another embodiment, thecement composition has a thickening time of at least 3 hours at thebottomhole temperature and pressure of the subterranean formation.

In one embodiment, the cement composition has an initial setting time ofless than 24 hours at a temperature of 220° F. (104° C.) and a pressureof 3,000 psi (21 MPa). In another embodiment, the cement composition hasan initial setting time of less than 24 hours at the bottomholetemperature and pressure of the subterranean formation.

Preferably, the cement composition has a setting time of less than 48hours at a temperature of 220° F. (104° C.). More preferably, the cementcomposition has a setting time of less than 24 hours at a temperature of220° F. (104° C.). Most preferably, the cement composition has a settingtime in the range of about 3 to about 24 hours at a temperature of 220°F. (104° C.). In another embodiment, the cement composition has asetting time of less than 48 hours at the bottomhole temperature andpressure of the subterranean formation.

Preferably, the cement composition has a non-destructive compressivestrength of at least 500 psi (3.5 MPa) when tested at 24 hours, atemperature of 220° F. (104° C.), and a pressure of 3,000 psi (21 MPa).More preferably, the cement composition has a non-destructivecompressive strength in the range of about 500 to about 10,000 psi(about 3.5 to about 69 MPa) when tested at 24 hours, a temperature of220° F. (104° C.), and a pressure of 3,000 psi (21 MPa).

The cement composition can further include an additive. Examples of anadditive include, but are not limited to, a filler, a fluid lossadditive, a set retarder, a friction reducer, a strength-retrogressionadditive, a defoaming agent, a high-density additive, a set accelerator,a mechanical property enhancing additive, a lost-circulation material, afiltration-control additive, a thixotropic additive, a nano-particle,and combinations thereof.

The cement composition can include a filler. Suitable examples offillers include, but are not limited to, fly ash, sand, clays, andvitrified shale. Preferably, the filler is in a concentration in therange of about 5% to about 50% by weight of the cement (bwc).

The cement composition can include a fluid loss additive. Suitableexamples of commercially-available fluid loss additives include, but arenot limited to, HALAD®-344, HALAD®-413, and HALAD®-300, marketed byHalliburton Energy Services, Inc. Preferably, the fluid loss additive isin a concentration in the range of about 0.05% to about 10% bwc.

The cement composition can include a set retarder. Suitable examples ofcommercially-available set retarders include, but are not limited to,HR®-4, HR®-5, HR®-6, HR®-12, HR®-20, HR®-25, SCR-100™, and SCR-500™,marketed by Halliburton Energy Services, Inc. Preferably, the setretarder is in a concentration in the range of about 0.05% to about 10%bwc.

The cement composition can include a friction reducer. Suitable examplesof commercially-available friction reducers include, but are not limitedto, CFR-2™, CFR-3™, CFR-5LE™, CFR-6™, and CFR-8™, marketed byHalliburton Energy Services, Inc. Preferably, the friction reducer is ina concentration in the range of about 0.1% to about 10% bwc.

The cement composition can include a strength-retrogression additive.Suitable examples of commercially-available strength-retrogressionadditives include, but are not limited to, SSA-1™ and SSA-2™, marketedby Halliburton Energy Services, Inc. Preferably, thestrength-retrogression additive is in a concentration in the range ofabout 5% to about 50% bwc.

Commercially-available examples of other additives include, but are notlimited to, High Dense® No. 3, High Dense® No. 4, Barite™, Micromax™,Silicalite™, WellLife® 665, WellLife® 809, WellLife® 810, and ChannelSeal™ Fluid, marketed by Halliburton Energy Services, Inc.

In one embodiment, the cement composition has a density of at least 10pounds per gallon (ppg) (1.2 kilograms per liter (kg/l)). In anotherembodiment, the cement composition has a density of at least 15 ppg (1.8kg/l). In another embodiment, the cement composition has a density inthe range of about 15 to about 20 ppg (about 1.8 to about 2.4 kg/l).

According to another embodiment, a method of cementing in a subterraneanformation comprises: introducing a cement composition into thesubterranean formation, wherein the cement composition comprises: (A)cement; (B) water; and (C) the surfactant; and allowing the cementcomposition to set.

The method embodiments include the step of introducing the cementcomposition into a subterranean formation. The step of introducing isfor the purpose of at least one of the following: well completion; foamcementing; primary or secondary cementing operations; well-plugging; andgravel packing. The cement composition can be in a pumpable state beforeand during introduction into the subterranean formation. In oneembodiment, the subterranean formation is penetrated by a well. The wellcan be an oil, gas, water, or injection well. According to thisembodiment, the step of introducing includes introducing the cementcomposition into the well. According to another embodiment, thesubterranean formation is penetrated by a well and the well includes anannulus. According to this other embodiment, the step of introducingincludes introducing the cement composition into a portion of theannulus.

Preferably, the method further includes the step of introducing anoil-based drilling mud into the subterranean formation prior to the stepof introducing the cement composition. According to this embodiment, thecement composition becomes contaminated with a hydrocarbon liquid fromthe oil-based drilling fluid at a concentration of about 2% to about 25%by volume of the cement composition. The method can further include thestep of introducing a spacer fluid into the subterranean formation priorto the step of introducing the cement composition. The method canfurther include the step of introducing the spacer fluid after the stepof introducing an oil-based drilling fluid into the subterraneanformation.

The method embodiments also include the step of allowing the cementcomposition to set. The step of allowing can be after the step ofintroducing the cement composition into the subterranean formation. Themethod can include the additional steps of perforating, fracturing, orperforming an acidizing treatment, after the step of allowing.

EXAMPLES

To facilitate a better understanding of the preferred embodiments, thefollowing examples of certain aspects of the preferred embodiments aregiven. The following examples are not the only examples that could begiven according to the preferred embodiments and are not intended tolimit the scope of the invention.

For the data contained in the following tables and figures, theconcentration of any ingredient in a cement composition or a drillingmud can be expressed as by weight of the cement (abbreviated as “bwc”);pounds per barrel (abbreviated as “lb/bbl”); or gallons per sack ofcement (abbreviated as “gal/sk”). Stabilizer 434D™ surfactant is anon-ionic surfactant of a substituted ethoxylated phenol. SurfactantMixtures 1 and 2 were a mixture of two different cardanol ethoxylates.Cardanol ethoxylate A (shown below) had 8 moles of ethylene oxide andcardanol ethoxylate B (shown below) had 13 moles of ethylene oxide,where m=0, 2, 4, and 6. Surfactant Mixture 1 was a mixture of 1 partcardanol ethoxylate A to 2 parts cardanol ethoxylate B, by volume.Surfactant Mixture 2 was a mixture of 2 parts cardanol ethoxylate A to 1part cardanol ethoxylate B, by volume.

Unless otherwise stated, each of the oil-based drilling muds had adensity of 13 pounds per gallon (lb/gal), had an oil water ratio of70:30, and contained the following ingredients: 0.17 lb/bbl BAROID®-41weighting agent; 0.51 lb/bbl of a specified hydrocarbon liquid; 0.255lb/bbl calcium chloride; 0.003 lb/bbl ADAPTA® fluid loss agent; 0.01lb/bbl BARACARB®-5 weighting agent; 0.025 lb/bbl LE SUPERMUL™emulsifier; 0.0007 lb/bbl RHEMOD™ L rheology modifier; and 0.022 lb/bblRev Dust drilling solids.

Unless otherwise stated, each of the cement compositions had a densityof 15.8 lb/gal and contained at least the following ingredients: 4.92gal/sk deionized water; Class G cement; 0.05 gal/sk D-AIR 3000L™defoaming agent; 1% bwc HALAD®-344 fluid loss additive; 0.8% bwcHALAD®-413 fluid loss additive; and 0.5% bwc SCR-100™ set retarder. Someof the cement compositions also included a surfactant.

Unless stated otherwise, all of the cement compositions were mixed andtested according to the procedure for the specific test as described inThe Detailed Description section above. Rheology testing was conductedat a temperature of 190° F. (88° C.). The cement compositions weretested for initial setting time at a temperature of 220° F. (104° C.)and a pressure of 3,000 psi (7 MPa). The tests for time to reach 500 psiwere conducted using the non-destructive compressive strength method ata temperature of 220° F. (104° C.) and a pressure of 3,000 psi (21 MPa).The non-destructive compressive strength tests were conducted at 24 or48 hours, a temperature of 220° F. (104° C.), and a pressure of 3,000psi (21 MPa). The thickening time tests were conducted at a temperatureof 185° F. (85° C.) and a pressure of 17,500 psi (121 MPa). The controlbase cement compositions did not include an oil-based drilling mud or asurfactant. Unless otherwise stated, the control contaminated basecement compositions included an oil-based drilling mud at aconcentration of 20% by volume of the cement compositions.

Table 1 contains initial setting time, time to 500 psi, non-destructivecompressive strength, and destructive compressive strength data forseveral cement compositions. The oil-based drilling mud was preparedwith ENCORE® drilling fluid (an internal olefin) as the hydrocarbonliquid. As can be seen in Table 1, the control contaminated base cementhad a much lower non-destructive and destructive compressive strengthcompared to the control base cement composition. As can also be seen inTable 1, the cement compositions containing Surfactant Mixtures 1 and 2exhibited shorter initial setting time and time to 500 psi, and alsoexhibited higher non-destructive compressive strengths compared to thecontrol contaminated base cement composition and the cement compositioncontaining Stabilizer 434D™. The data in Table 1 shows that cardanolethoxylate performs better than Stabilizer 434D™ (which is a substitutedethoxylated phenol).

TABLE 1 Non- Initial Destructive Destructive Conc. of Mud Set Time toComp. Strength Comp. Type of Surfactant Contamination Time 500 psi 24 hr48 hr Strength Surfactant (% bwc) (% by Vol) (hr:min) (hr:min) (psi)(psi) (psi) Ctl. Base 0 0 10:22 11:00 2350 2574 5180 Cement Ctl. 0 2010:05 14:06 769 835 1101 Contaminated Base Cement Stabilizer 2 20  9:0711:44 1004 1168 — 434D ™ Stabilizer 0.9 20 10:01 22:16 531.6 — — 434D ™Surfactant 0.9 20  8:11 10:34 1143.7 — — Mixture 1 Surfactant 0.9 20 8:34 10:38 1194 — — Mixture 2

Table 2 contains rheology, initial setting time, time to 500 psi, andnon-destructive compressive strength data for several cementcompositions. The oil-based drilling mud was prepared with ENCORE®drilling fluid (an internal olefin) as the hydrocarbon liquid. As can beseen in Table 2, the three cement compositions containing a surfactantexhibited better rheologies and comparable initial setting time comparedto both, the control base cement composition and the controlcontaminated base cement composition. As can also be seen in Table 2,the cement compositions containing Surfactant Mixtures 1 and 2 exhibitedcomparable time to 500 psi compared to the control base cementcomposition, and higher non-destructive compressive strength compared tothe control contaminated base cement composition and the cementcomposition containing Stabilizer 434D™.

TABLE 2 Initial Non-D Conc. Set Time to Comp. Type of of Surf. RheologyTime 500 psi Str. 24 hr Surfactant (% bwc) 3 6 30 60 100 200 300 600(hr:min) (hr:min) (psi) Ctl. Base 0 11 19 67 111 160 265 +300 +300 10:2211:00 2350 Cement Ctl. 0 23 36 55 85 140 200 +300 +300 10:05 14:06 769Contaminated Base Cement Stabilizer 0.9 4 7 25 45 68 105 145 234 10:0122:16 531.6 434D ™ Surf. 0.9 10 15 4 54 72 104 142 +300  8:11 10:341143.7 Mixture 1 Surf. 0.9 12 16 48 55 75 115 149 +300  8:34 10:38 1194Mixture 2

Table 3 contains rheology, initial setting time, time to 500 psi, andnon-destructive compressive strength data for several cementcompositions. The oil-based drilling mud was prepared with ESCAID 110™(a mineral oil blend of mainly alkanes and cyclic alkanes) as thehydrocarbon liquid. As can be seen in Table 3, the two cementcompositions containing a surfactant exhibited better rheologies andshorter initial setting time compared to both, the control base cementcomposition and the control contaminated base cement composition. As canalso be seen in Table 3, the cement composition containing SurfactantMixture 1 exhibited a higher non-destructive compressive strengthcompared to the control contaminated base cement composition and thecement composition containing Stabilizer 434D™.

TABLE 3 Initial Non-D Conc. Set Time to Comp. Type of of Surf. RheologyTime 500 psi Str. 24 hr Surfactant (% bwc) 3 6 30 60 100 200 300 600(hr:min) (hr:min) (psi) Ctl. Base 0 11 19 67 111 160 265 +300 +300 10:2211:00 2350 Cement Ctl. 0 15 28 75 108 141 211 270 +300 11:10 16:12 742.2Contaminated Base Cement Stabilizer 0.9 2 3 7 12 19 52 96 191  8:25 —316.5 434D ™ Surf. 0.9 6 10 29 45 62 102 138 248  9:29 12:27 1017.8Mixture 1

Table 4 contains rheology, initial setting time, time to 500 psi, andnon-destructive compressive strength data for several cementcompositions. The oil-based drilling mud was prepared with PETROFREE®ESTER base fluid (a fatty acid ester) as the hydrocarbon liquid. As canbe seen in Table 4, the two cement compositions containing a surfactantexhibited better rheologies and comparable initial setting time comparedto both, the control base cement composition and the controlcontaminated base cement composition. As can also be seen in Table 4,the cement composition containing Surfactant Mixture 1 exhibited ahigher non-destructive compressive strength compared to the controlcontaminated base cement composition and the cement compositioncontaining Stabilizer 434D™.

TABLE 4 Initial Non-D Conc. Set Time to Comp. Type of of Surf. RheologyTime 500 psi Str. 24 hr Surfactant (% bwc) 3 6 30 60 100 200 300 600(hr:min) (hr:min) (psi) Ctl. Base 0 11 19 67 111 160 265 +300 +30010:22  11:00 2350 Cement Ctl. 0 20 34 89 128 165 234 +300 +300 9:36 —351.2 Contaminated Base Cement Stabilizer 0.9 15 20 43 50 70 95 114 1849:40 — 207.5 434D ™ Surf. 0.9 8 11 24 38 50 78 105 248 9:54 — 419.4Mixture 1

Table 5 contains rheology, initial setting time, time to 500 psi, andnon-destructive compressive strength data for several cementcompositions. The oil-based drilling mud was prepared with XP-07™ basefluid (a synthetic paraffin) as the hydrocarbon liquid. As can be seenin Table 5, the two cement compositions containing a surfactantexhibited better rheologies and comparable initial setting time comparedto both, the control base cement composition and the controlcontaminated base cement composition. As can also be seen in Table 5,the cement composition containing Surfactant Mixture 1 exhibited ashorter time to 500 psi and a higher non-destructive compressivestrength compared to the control contaminated base cement composition.

TABLE 5 Initial Non-D Conc. Set Time to Comp. Type of of Surf. RheologyTime 500 psi Str. 24 hr Surfactant (% bwc) 3 6 30 60 100 200 300 600(hr:min) (hr:min) (psi) Ctl. Base 0 11 19 67 111 160 265 +300 +300 10:2211:00 2350 Cement Ctl. 0 12 16 45 80 111 165 240 +300 11:37 20:04 581.7Contaminated Base Cement Stabilizer 0.9 8 11 25 30 36 53 74 132  9:3816:36 677.7 434D ™ Surf. 0.9 10 15 20 32 40 70 95 195 11:33 17:46 648.3Mixture 1

The tests for the data listed in Table 6 were conducted to evaluate theeffectiveness of Surfactant Mixture 1 with varying degrees of mudcontamination. The cement compositions contained varying amounts of anoil-based drilling mud containing ESCAID 110™ as the hydrocarbon liquidand contained varying amounts of Surfactant Mixture 1. Table 6 containsrheology, initial setting time, time to 500 psi, and non-destructivecompressive strength data for several cement compositions. As can beseen in Table 6, for a given concentration of mud contamination, thecement compositions containing Surfactant Mixture 1 exhibited better orcomparable rheologies, shorter or comparable initial setting time andtime to 500 psi, and higher non-destructive compressive strength,compared to the cement compositions that did not include SurfactantMixture 1. As can also be seen in Table 6, Surfactant Mixture 1increased the compressive strength of a contaminated cement compositioncompared to a contaminated cement composition without the surfactant. Asa result, it appears that Surfactant Mixture 1 has applications in awide variety of wells with varying degrees of oil-based mudcontamination.

TABLE 6 Initial Non-D Conc. of Conc. Set Time to Comp. Mud (% by ofSurf. Rheology Time 500 psi Str. 24 hr Vol) (% bwc) 3 6 30 60 100 200300 600 (hr:min) (hr:min) (psi) 0 0 11 19 67 111 160 265 +300 +30010:22  11:00 2350 15 0 8 12 27 49 74 147 210 +300 9:47 15:46 735.6 0.9 913 41 63 92 153 210 +300 9:49 12:17 1000.7 20 0 15 25 75 108 141 211 270+300 11:10  16:12 742.2 0.9 6 10 29 45 62 102 138 248 9:29 12:27 1017.825 0 15 26 73 112 153 243 +300 +300 9:41 — 403.8 0.9 16 28 84 120 182276 +300 +300 10:22  15:41 706.4

As can be seen in Tables 1-6, Surfactant Mixtures 1 and 2, andStabilizer 434D™ are suitable for use with a variety of oil-baseddrilling muds. When the hydrocarbon liquid for the oil-based drillingmud was an internal olefin or a mineral oil blend of mainly alkanes andcyclic alkanes, Surfactant Mixture 1 provided a much greater increase inthe compressive strength of the cement composition compared to thecontrol contaminated cement compositions. When the hydrocarbon liquidfor the oil-based drilling fluid was a fatty acid ester or a paraffin,Surfactant Mixture 1 provided a smaller increase in the compressivestrength of the cement composition compared to the control contaminatedcement compositions.

Table 7 contains thickening time data and time to reach 100 Bc data forthree different cement compositions. The oil-based drilling mud wasprepared with ENCORE® drilling fluid as the hydrocarbon liquid. As canbe seen in Table 7, the cement composition containing the surfactantexhibited a comparable thickening time and time to reach 100 Bc comparedto the control contaminated cement composition, and exhibited a slightlyshorter thickening time and time to reach 100 Bc compared to the controlbase cement composition.

TABLE 7 Conc. of Thickening Time to Surfactant Time Reach 100 Bc Type ofSurfactant (% bwc) (hr:min) (hr:min) Ctl. Base Cement   0 7:06 7:11 Ctl.Contaminated Base Cement   0 6:27 6:27 Surfactant Mixture 1 0.9 6:236:32

Therefore, the present invention is well adapted to attain the ends andadvantages mentioned as well as those that are inherent therein. Theparticular embodiments disclosed above are illustrative only, as thepresent invention may be modified and practiced in different butequivalent manners apparent to those skilled in the art having thebenefit of the teachings herein. Furthermore, no limitations areintended to the details of construction or design herein shown, otherthan as described in the claims below. It is, therefore, evident thatthe particular illustrative embodiments disclosed above may be alteredor modified and all such variations are considered within the scope andspirit of the present invention. While compositions and methods aredescribed in terms of “comprising,” “containing,” or “including” variouscomponents or steps, the compositions and methods also can “consistessentially of” or “consist of” the various components and steps.Whenever a numerical range with a lower limit and an upper limit isdisclosed, any number and any included range falling within the range isspecifically disclosed. In particular, every range of values (of theform, “from about a to about b,” or, equivalently, “from approximately ato b,” or, equivalently, “from approximately a to b”) disclosed hereinis to be understood to set forth every number and range encompassedwithin the broader range of values. Also, the terms in the claims havetheir plain, ordinary meaning unless otherwise explicitly and clearlydefined by the patentee. Moreover, the indefinite articles “a” or “an”,as used in the claims, are defined herein to mean one or more than oneof the element that it introduces. If there is any conflict in theusages of a word or term in this specification and one or more patent(s)or other documents that may be incorporated herein by reference, thedefinitions that are consistent with this specification should beadopted.

What is claimed is:
 1. A well treatment composition comprising: cement;water; and a surfactant comprising: a substituted ethoxylated phenol andderivatives thereof, having at least one substituent, wherein thesubstituted ethoxylated phenol and derivatives thereof comprises atleast one of the following chemical structures:

where n=1-14, R=an alkyl, alkene, or alkyne with a carbon chain lengthin the range of 4 to 25, and where m=0, 2, 4, and 6; wherein thesubstituted ethoxylated phenol and derivatives thereof, is a substitutedcardanol ethoxylate and wherein the substituted cardanol ethoxylate andderivatives thereof has at least one of the following chemicalstructures:

where n=1-14; m=0, 2, 4, and 6; and R₁=an alkyl, alkene, or alkyne witha carbon chain length in the range of 4 to
 25. 2. The compositionaccording to claim 1, wherein the cement is selected from the groupconsisting of Class A cement, Class C cement, Class G cement, Class Hcement, and any combination thereof.
 3. The composition according toclaim 1, wherein the water is selected from the group consisting offreshwater, brackish water, saltwater, and any combination thereof. 4.The composition according to claim 1, wherein the surfactant isnon-ionic.
 5. The composition according to claim 1, wherein thesurfactant comprises a para-substituted ethoxylated phenol derivative inwhich R=an alkyl with a carbon chain length of
 9. 6. The compositionaccording to claim 1, wherein n=6-13.
 7. The composition according toclaim 1, wherein the surfactant is biodegradable.
 8. The compositionaccording to claim 1, wherein the surfactant is in a concentration inthe range of about 0.05% to about 5% by weight of the cement.
 9. Thecomposition according to claim 1, wherein the composition has athickening time in the range of about 4 to about 15 hours at atemperature of 185° F. (88° C.) and a pressure of 17,500 psi (121 MPa).10. The composition according to claim 1, wherein the composition has aninitial setting time of less than 24 hours at a temperature of 220° F.(104° C.) and a pressure of 3,000 psi (21 MPa).
 11. The compositionaccording to claim 1, wherein the composition has a setting time of lessthan 48 hours at a temperature of 220° F. (104° C.).
 12. The compositionaccording to claim 1, wherein the composition has a non-destructivecompressive strength in the range of about 500 to about 10,000 psi(about 3.5 to about 69 MPa) when tested at 24 hours, a temperature of220° F. (104° C.), and a pressure of 3,000 psi (21 MPa).
 13. Thecomposition according to claim 1, wherein the composition has an initialsetting time of less than 24 hours at the bottomhole temperature andpressure of a subterranean formation.
 14. The composition according toclaim 1, wherein the composition has a setting time of less than 48hours at the bottomhole temperature and pressure of a subterraneanformation.
 15. The composition according to claim 1, wherein thecomposition has a non-destructive compressive strength in the range ofabout 500 to about 10,000 psi (about 3.5 to about 69 MPa) the bottomholetemperature and pressure of a subterranean formation.
 16. Thecomposition according to claim 1, wherein the composition furtherincludes an additive.
 17. The composition according to claim 15, whereinthe additive is selected from the group consisting of a filler, a fluidloss additive, a set retarder, a friction reducer, astrength-retrogression additive, a defoaming agent, a high-densityadditive, a set accelerator, a mechanical property enhancing additive, alost-circulation material, a filtration-control additive, a thixotropicadditive, a nano-particle, and combinations thereof.
 18. The compositionaccording to claim 1, wherein the composition has a density in the rangeof about 15 to about 20 ppg (about 1.8 to about 2.4 kg/l).
 19. Thecomposition according to claim 17, wherein the composition becomescontaminated with a hydrocarbon liquid from an oil-based drilling fluidat a concentration of about 2% to about 25% by volume of thecomposition.